Binding SnO2 Nanoparticles with MoS2 Nanosheets Toward Highly Reversible and Cycle‐Stable Lithium/Sodium Storage

Author:

Cheng Deliang12,Zhang Wenbiao3,Tang Yi4,Gao Qingsheng3,Hu Renzong2ORCID,Yang Lichun2ORCID,Zhu Min2ORCID

Affiliation:

1. Institute of Advanced Materials Jiangxi Normal University Nanchang 330022 China

2. School of Materials Science and Engineering Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials South China University of Technology Guangzhou 510641 China

3. College of Chemistry and Materials Science Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications Jinan University Guangzhou 510632 China

4. Department of Chemistry Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Laboratory of Advanced Materials and Collaborative Innovation Center of Chemistry for Energy Materials Fudan University Shanghai 200433 China

Abstract

SnO2, with its high theoretical capacity, abundant resources, and environmental friendliness, is widely regarded as a potential anode material for lithium‐ion batteries (LIBs). Nevertheless, the coarsening of the Sn nanoparticles impedes the reconversion back to SnO2, resulting in low coulombic efficiency and rapid capacity decay. In this study, we fabricated a heterostructure by combining SnO2 nanoparticles with MoS2 nanosheets via plasma‐assisted milling. The heterostructure consists of in‐situ exfoliated MoS2 nanosheets predominantly in 1 T phase, which tightly encase the SnO2 nanoparticles through strong bonding. This configuration effectively mitigates the volume change and particle aggregation upon cycling. Moreover, the strong affinity of Mo, which is the lithiation product of MoS2, toward Sn plays a pivotal role in inhibiting the coarsening of Sn nanograins, thus enhancing the reversibility of Sn to SnO2 upon cycling. Consequently, the SnO2/MoS2 heterostructure exhibits superb performance as an anode material for LIBs, demonstrating high capacity, rapid rate capability, and extended lifespan. Specifically, discharged/charged at a rate of 0.2 A g−1 for 300 cycles, it achieves a remarkable reversible capacity of 1173.4 mAh g−1. Even cycled at high rates of 1.0 and 5.0 A g−1 for 800 cycles, it still retains high reversible capacities of 1005.3 and 768.8 mAh g−1, respectively. Moreover, the heterostructure exhibits outstanding electrochemical performance in both full LIBs and sodium‐ion batteries.

Funder

National Basic Research Program of China

Natural Science Foundation of Jiangxi Province

Publisher

Wiley

Subject

Energy (miscellaneous),Waste Management and Disposal,Environmental Science (miscellaneous),Water Science and Technology,General Materials Science,Renewable Energy, Sustainability and the Environment

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